New purpose of N-(2)-L-alanyl-L-glutamine
A glutamate dipeptide, pharmaceutical technology, applied in the field of biomedicine to achieve the effect of increasing the diameter of the femur, reducing the blood calcium concentration, and reducing the length of the femur
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Embodiment 1
[0014] Effects of glucodipeptide on changes in femur length and diameter in rats induced by weightlessness
[0015] This embodiment provides a dosage form of dipeptide injection, which includes a dipeptide main body and a drug carrier. Wherein, the main body of dipipeptide is a composition containing one or more of dipeptide and pharmaceutically acceptable salts, esters, and solvates thereof. Wherein, the carrier includes water, physiological saline, phosphate buffer saline, bacteriostatic water, ethanol, polyalcohol and mixture thereof, as well as liposome and polymer nanoparticle. These compositions must be sterile and liquid injectables.
[0016] The experimental method is as follows:
[0017] (1) Construction of rat model of osteoporosis caused by weightlessness: SPF grade male SD rats were selected, and all rats were kept in independent cages. After the tail was cleaned, both sides of the tail of the rat were pasted with medical air-permeable adhesive tape. Then connec...
Embodiment 2
[0024] Effects of glucodipeptide on the changes of blood calcium index in rats induced by weightlessness
[0025] The experimental method is as follows:
[0026] (1) Construction of rat model of osteoporosis caused by weightlessness: same as Example 1;
[0027] (2) Rat model grouping and drug treatment: same as in Example 1.
[0028] The experimental results are as follows (Table 2): the measured ionized calcium concentration and total calcium concentration of the rats in the blank control group were 1.21±0.05 mmol / L and 2.37±0.04 mmol / L, respectively; The total calcium concentration was 1.23±0.03 mmol / L and 2.46±0.03 mmol / L, respectively; the measured ionized calcium concentration and total calcium concentration of the rats administered with dipeptide were 1.16±0.02 mmol / L and 2.33±0.03 mmol / L, respectively. Compared with the tail-suspension model group, the measured ionized calcium concentration and total calcium concentration of the rats in the dipeptide-administered grou...
Embodiment 3
[0033] Provide a kind of dipeptide tablet
[0034] The present embodiment provides a kind of dipeptide tablet, the formula is as follows: dipeptide or its salt or ester 50 g, microcrystalline cellulose 50 g, lactose 28 g, calcium hydrogen phosphate 10 g, croscarmellose sodium 5 g , 2 g of magnesium stearate, appropriate amount of purified water. Make 1000 proglu dipeptide or its salt or ester tablet.
[0035] The preparation process is as follows:
[0036] 1. Glycine dipeptide or its salt or ester is crushed through an 80-mesh sieve and set aside;
[0037] 2. Lactose passed through a 60-mesh sieve, set aside;
[0038] 3. Fully mix 1 and 2 with microcrystalline cellulose, calcium hydrogen phosphate, and croscarmellose sodium;
[0039] 4. Use water to make soft material, granulate with 20 mesh sieve, dry at 60 degrees, and granulate with 24 mesh sieve;
[0040] 5. Add magnesium stearate, mix well, and press into tablets.
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